mA Regulates Neurogenesis and Neuronal Development by Modulating Histone Methyltransferase Ezh2.
10.1016/j.gpb.2018.12.007
- Author:
Junchen CHEN
1
,
2
;
Yi-Chang ZHANG
3
,
4
,
5
;
Chunmin HUANG
6
;
Hui SHEN
1
,
2
;
Baofa SUN
3
,
4
,
7
,
8
;
Xuejun CHENG
1
,
2
;
Yu-Jie ZHANG
9
;
Yun-Gui YANG
3
,
4
,
7
,
8
;
Qiang SHU
10
;
Ying YANG
3
,
4
,
7
,
11
;
Xuekun LI
1
,
12
Author Information
1. The Children's Hospital, School of Medicine, Zhejiang University, Hangzhou 310052, China
2. The Institute of Translational Medicine, School of Medicine, Zhejiang University, Hangzhou 310029, China.
3. CAS Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, College of Future Technology, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China
4. University of Chinese Academy of Sciences, Beijing 100049, China
5. Sino-Danish College, University of Chinese Academy of Sciences, Beijing 101408, China.
6. CAS Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, College of Future Technology, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
7. Sino-Danish College, University of Chinese Academy of Sciences, Beijing 101408, China
8. Institute of Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.
9. The Institute of Translational Medicine, School of Medicine, Zhejiang University, Hangzhou 310029, China.
10. The Children's Hospital, School of Medicine, Zhejiang University, Hangzhou 310052, China. Electronic address: shuqiang@zju.edu.cn.
11. Institute of Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China. Electronic address: yingyang@big.ac.cn.
12. The Institute of Translational Medicine, School of Medicine, Zhejiang University, Hangzhou 310029, China. Electronic address: xuekun_li@zju.edu.cn.
- Publication Type:Journal Article
- Keywords:
Ezh2;
Mettl3;
N(6)-methyladenosine (m(6)A);
Neurogenesis;
Neuronal development
- MeSH:
Adenosine;
analogs & derivatives;
metabolism;
Adult Stem Cells;
cytology;
metabolism;
Animals;
Brain;
metabolism;
Cell Differentiation;
genetics;
Cell Proliferation;
Enhancer of Zeste Homolog 2 Protein;
metabolism;
Gene Expression Regulation;
Methyltransferases;
metabolism;
Mice, Inbred C57BL;
Neural Stem Cells;
cytology;
metabolism;
Neurogenesis;
genetics;
Neurons;
cytology;
metabolism;
RNA, Messenger;
genetics;
metabolism
- From:
Genomics, Proteomics & Bioinformatics
2019;17(2):154-168
- CountryChina
- Language:English
-
Abstract:
N-methyladenosine (mA), catalyzed by the methyltransferase complex consisting of Mettl3 and Mettl14, is the most abundant RNA modification in mRNAs and participates in diverse biological processes. However, the roles and precise mechanisms of mA modification in regulating neuronal development and adult neurogenesis remain unclear. Here, we examined the function of Mettl3, the key component of the complex, in neuronal development and adult neurogenesis of mice. We found that the depletion of Mettl3 significantly reduced mA levels in adult neural stem cells (aNSCs) and inhibited the proliferation of aNSCs. Mettl3 depletion not only inhibited neuronal development and skewed the differentiation of aNSCs more toward glial lineage, but also affected the morphological maturation of newborn neurons in the adult brain. mA immunoprecipitation combined with deep sequencing (MeRIP-seq) revealed that mA was predominantly enriched in transcripts related to neurogenesis and neuronal development. Mechanistically, mA was present on the transcripts of histone methyltransferase Ezh2, and its reduction upon Mettl3 knockdown decreased both Ezh2 protein expression and consequent H3K27me3 levels. The defects of neurogenesis and neuronal development induced by Mettl3 depletion could be rescued by Ezh2 overexpression. Collectively, our results uncover a crosstalk between RNA and histone modifications and indicate that Mettl3-mediated mA modification plays an important role in regulating neurogenesis and neuronal development through modulating Ezh2.
